Girls aged 2-9 who have Lightheadedness with Humatrope - from FDA reports

A study for girls aged 2-9 who have Lightheadedness while taking Humatrope. This study is created by eHealthMe based on reports of 206 people who have side effects when taking Lipitor from FDA, and is updated regularly.

How to use this study: bring a copy to your health teams to ensure drug risks and benefits are fully discussed and understood.

On Feb, 11, 2019

206 girls aged 2-9 reported to have side effects when taking Humatrope.
Among them, 2 people (0.97%) have Lightheadedness

Number of reports submitted per year:

Could Humatrope cause Lightheadedness?

Top other side effects for these people *:

  1. Vestibular Disorder (disorders of the body's balance (vestibular) system in the inner ear): 1 person, 50.00%
  2. Nausea (feeling of having an urge to vomit): 1 person, 50.00%
  3. Meniere's Disease (a disorder of the inner ear that can affect hearing and balance to a varying degree): 1 person, 50.00%
  4. Injection Site Pain: 1 person, 50.00%
  5. Hypoacusis (loss of hearing): 1 person, 50.00%
  6. Fever: 1 person, 50.00%
  7. Deafness Neurosensory: 1 person, 50.00%

* Approximation only. Some reports may have incomplete information.

Do you have Lightheadedness while taking Humatrope?

You are not alone:

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Who have Lightheadedness with Humatrope?

What would happen?

Predict new side effects and undetected conditions when you take Humatrope and have Lightheadedness

Recent updates

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NOTE: The study is based on active ingredients and brand name. Other drugs that have the same active ingredients (e.g. generic drugs) are NOT considered.

WARNING: Please DO NOT STOP MEDICATIONS without first consulting a physician since doing so could be hazardous to your health.

DISCLAIMER: All material available on is for informational purposes only, and is not a substitute for medical advice, diagnosis, or treatment provided by a qualified healthcare provider. All information is observation-only, and has not been supported by scientific studies or clinical trials unless otherwise stated. Different individuals may respond to medication in different ways. Every effort has been made to ensure that all information is accurate, up-to-date, and complete, but no guarantee is made to that effect. The use of the eHealthMe site and its content is at your own risk.

You may report adverse side effects to the FDA at or 1-800-FDA-1088 (1-800-332-1088).

If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.

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